rs2615374
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2615374(A;A) |
Make rs2615374(A;G) |
Make rs2615374(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 139618747 |
Gene | KCNK9 |
is a | snp |
is | mentioned by |
dbSNP | rs2615374 |
dbSNP (classic) | rs2615374 |
ClinGen | rs2615374 |
ebi | rs2615374 |
HLI | rs2615374 |
Exac | rs2615374 |
Gnomad | rs2615374 |
Varsome | rs2615374 |
LitVar | rs2615374 |
Map | rs2615374 |
PheGenI | rs2615374 |
Biobank | rs2615374 |
1000 genomes | rs2615374 |
hgdp | rs2615374 |
ensembl | rs2615374 |
geneview | rs2615374 |
scholar | rs2615374 |
rs2615374 | |
pharmgkb | rs2615374 |
gwascentral | rs2615374 |
openSNP | rs2615374 |
23andMe | rs2615374 |
SNPshot | rs2615374 |
SNPdbe | rs2615374 |
MSV3d | rs2615374 |
GWAS Ctlg | rs2615374 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24980697] Screening individuals with intellectual disability, autism and Tourette's syndrome for KCNK9 mutations and aberrant DNA methylation within the 8q24 imprinted cluster